HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107701128A>T , CM000669.2:g.107701128A>T | GRCh38 |
NC_000007.13:g.107341573A>T , CM000669.1:g.107341573A>T | GRCh37 |
NC_000007.12:g.107128809A>T | NCBI36 |
NG_008489.1:g.45494A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644269.2:c.1735A>T MANE Select | ENSP00000494017.1:p.Asn579Tyr | |
ENST00000644846.1:c.446A>T | ||
ENST00000265715.7:c.1735A>T | ENSP00000265715.3:p.Asn579Tyr | |
ENST00000480841.5:n.584A>T | ||
ENST00000492030.2:n.91-699A>T | ||
NM_000441.1:c.1735A>T | NP_000432.1:p.Asn579Tyr | |
XM_005250425.1:c.1735A>T | XP_005250482.1:p.Asn579Tyr | |
XM_005250425.2:c.1735A>T | XP_005250482.1:p.Asn579Tyr | |
XM_017012318.1:c.1657A>T | XP_016867807.1:p.Asn553Tyr | |
NM_000441.2:c.1735A>T MANE Select | NP_000432.1:p.Asn579Tyr |